FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GENERATOR, OXYGEN, PORTABLE
K Number: K780020
·
Decision Jan 26, 1978
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
286
Applicant Total
2
Review Days
23
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Basic Information
- Device Name
- GENERATOR, OXYGEN, PORTABLE
- K Number
- K780020
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5440
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Jet Research Center, Inc.
- Date Received
- January 3, 1978
- Decision Date
- January 26, 1978
- Product Code
- CAW
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| CAW | Generator, Oxygen, Portable | FDA class 2 | Anesthesiology |
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Other Clearances by Jet Research Center, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K771761 | SOLID OXYGEN SYSTEM | Oct 4, 1977 | Substantially Equivalent |